Evidence map›Paper›PMID 33110476›Full record

ArticleOncotarget2020

Combination of copanlisib with cetuximab improves tumor response in cetuximab-resistant patient-derived xenografts of head and neck cancer.

Konrad Klinghammer, Oliver Politz, Theresa Eder, Raik Otto, Jan-Dirk Raguse, Andreas Albers, Andreas Kaufmann, Ingeborg Tinhofer, Jens Hoffmann, Ulrich Keller and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 1 country.

Konrad KlinghammerDepartment of Hematology and Medical Oncology, Charité, Berlin, Germany.
Oliver PolitzBayer AG, Research & Development, Pharmaceuticals, Berlin, Germany.
Theresa EderDepartment of Radiooncology and Radiotherapy, Charité University Hospital, Berlin, Germany.
Raik OttoWBI, Humboldt-Universität zu Berlin, Berlin, Germany.
Jan-Dirk RaguseDepartment of Maxillio-Facial Surgery, Fachklinik Hornheide, Münster, Germany.
Andreas AlbersDepartment of ENT, Charité, Berlin, Germany.
Andreas KaufmannDepartment of Gynaecology, Charité, Berlin, Germany.
Ingeborg TinhoferDepartment of Radiooncology and Radiotherapy, Charité University Hospital, Berlin, Germany.
Jens HoffmannExperimental Pharmacology & Oncology GmbH, Berlin, Germany.
Ulrich KellerDepartment of Hematology and Medical Oncology, Charité, Berlin, Germany.
Ulrich KeilholzCharité Comprehensive Cancer Center, Berlin, Germany.
Charité - Universitätsmedizin Berlin · DEBayer (Germany) · DEDeutschen Konsortium für Translationale Krebsforschung · DEFachklinik Hornheide · DEHumboldt-Universität zu Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite recent advances, the treatment of head and neck squamous cell carcinoma (HNSCC) remains an area of high unmet medical need. HNSCC is frequently associated with either amplification or mutational changes in the PI3K pathway, making PI3K an attractive target particularly in cetuximab-resistant tumors. Here, we explored the antitumor activity of the selective, pan-class I PI3K inhibitor copanlisib with predominant activity towards PI3Kα and δ in monotherapy and in combination with cetuximab using a mouse clinical trial set-up with 33 patient-derived xenograft (PDX) models with known HPV and PI3K mutational status and available data on cetuximab sensitivity. Treatment with copanlisib alone resulted in moderate antitumor activity with 12/33 PDX models showing either tumor stabilization or regression. Combination treatment with copanlisib and cetuximab was superior to either of the monotherapies alone in the majority of the models (21/33), and the effect was particularly pronounced in cetuximab-resistant tumors (14/16). While no correlation was observed between PI3K mutation status and response to either cetuximab or copanlisib, increased PI3K signaling activity evaluated through gene expression profiling showed a positive correlation with response to copanlisib. Together, these data support further investigation of PI3K inhibition in HNSCC and suggests gene expression patterns associated with PI3K signaling as a potential biomarker for predicting treatment responses.

Indexed as

cetuximabcopanlisibhead and neck squamous cell carcinomaHPVpatient-derived xenograft model

Identifiers

PMID33110476
PMCPMC7566806
OpenAlexW3097494231

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.